Wen Liu

发表

Implementation of the CYP Index for the Design of Selective Tryptophan-2,3-dioxygenase Inhibitors.

Benjamin D. Sellers, Rohan V Mendonca, Sanjeev Kumar, 2020, ACS medicinal chemistry letters.

Design, synthesis and biological evaluation of heterocyclic azoles derivatives containing pyrazine moiety as potential telomerase inhibitors.

Hai‐Liang Zhu, Yan-Bin Zhang, Yu-Shun Yang, 2012, Bioorganic & medicinal chemistry.

Triazole derivatives and their antiplasmodial and antimalarial activities.

Weiqi Wang, Cong Wang, Kun-lai Sun, 2019, European journal of medicinal chemistry.

A novel Gboxin analog induces OXPHOS inhibition and mitochondrial dysfunction-mediated apoptosis in diffuse large B-cell lymphoma.

Changxing Qi, Yonghui Zhang, Qingyi Tong, 2022, Bioorganic chemistry.

Aminoimidazoles as bioisosteres of acylguanidines: novel, potent, selective and orally bioavailable inhibitors of the sodium hydrogen exchanger isoform-1.

M. Kirby, Saleem Ahmad, G. Chandrasena, 2004, Bioorganic & medicinal chemistry letters.

Tryptamine and homotryptamine-based sulfonamides as potent and selective inhibitors of 15-lipoxygenase.

J. Macor, N. Murugesan, Z. Gu, 2005, Bioorganic & medicinal chemistry letters.

A new model of the tautomycin-PP1 complex that is not analogous to the corresponding okadaic acid structure.

A. Nairn, A. Chamberlin, Hsien-Bin Huang, 2003, Bioorganic & medicinal chemistry letters.

The selective inhibition of phosphatases by natural toxins: the anhydride domain of tautomycin is not a primary factor in controlling PP1/PP2A selectivity.

A. Nairn, A. Chamberlin, Hsien-Bin Huang, 2003, Bioorganic & medicinal chemistry letters.

Quinoline and quinolone dimers and their biological activities: An overview.

Chengying Zhao, Cong Wang, Wen Liu, 2019, European journal of medicinal chemistry.

Discovery of selective imidazole-based inhibitors of mammalian 15-lipoxygenase: highly potent against human enzyme within a cellular environment.

C. S. Madsen, Shaobin Zhuang, J. Robl, 2007, Bioorganic & medicinal chemistry letters.

Synthesis, molecular modeling, and biological evaluation of 1,2,4-triazole derivatives containing pyridine as potential anti-tumor agents

Yan-Bin Zhang, Yu-Shun Yang, Li-Fei Bai, 2012, Medicinal Chemistry Research.

Azaindole hydroxamic acids are potent HIV-1 integrase inhibitors.

A. Kuki, S. Butler, S. V. Rahavendran, 2009, Journal of medicinal chemistry.

Azaindole N-methyl hydroxamic acids as HIV-1 integrase inhibitors-II. The impact of physicochemical properties on ADME and PK.

A. Kuki, S. Butler, Buwen Huang, 2010, Bioorganic & medicinal chemistry letters.

Total Synthesis of the Serine/Threonine-Specific Protein Phosphatase Inhibitor Tautomycin(1).

A. Chamberlin, J. Sheppeck, Wen Liu, 1997, The Journal of organic chemistry.

Pyrazole-based sulfonamide and sulfamides as potent inhibitors of mammalian 15-lipoxygenase.

Saleem Ahmad, C. S. Madsen, Xing Chen, 2011, Bioorganic & medicinal chemistry letters.

3-Arylpropionylhydroxamic acid derivatives as Helicobacter pylori urease inhibitors: Synthesis, molecular docking and biological evaluation.

Hong-yu Zhang, Peng-Fei Wang, Meini Yang, 2016, Bioorganic & medicinal chemistry.